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United States · US · US:68180-403_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4
CEFPROZIL
Orange BookUNIISPLATC J01DC
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerLupin Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeJ01DC
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116818040301100 TABLET in 1 BOTTLE (68180-403-01)
Annotations
UNII (FDA Substance ID)
4W0459ZA4V
CEFPROZIL
RxCUI 19552
Orange Book
A065276
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4W0459ZA4V",
"rxcui": "19552",
"inchikey": null,
"display_name": "CEFPROZIL",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"800a2ec0-4798-4423-9613-d03024cf1f0e": {
"match": "brand_token",
"title": "CEFPROZIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.]",
"spl_version": "1",
"published_date": "2026-05-06"
}
},
"productid": "68180-403_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4",
"productndc": "68180-403",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "065276",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "250MG",
"product_no": "001",
"approval_date": "Dec 8, 2005"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "002",
"approval_date": "Dec 8, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CEFPROZIL",
"proprietary_name": "CEFPROZIL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA065276",
"marketing_category": "ANDA",
"nonproprietary_name": "CEFPROZIL",
"start_marketing_date": "20051201",
"active_numerator_strength": "250"
}Related drugs
Other records sharing ATC code J01DC.
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